Inhibition of human and woodchuck hepatitis virus DNA polymerase by the triphosphates of acyclovir, 1-(2′-deoxy-2′-fluoro-β-d-arabinofuranosyl)-5-iodocytosine and E-5-(2-bromovinyl)-2′-deoxyuridine
Author:
Publisher
Elsevier BV
Subject
Virology,Pharmacology
Reference28 articles.
1. Mode of action of acyclovir triphosphate on herpesviral and cellular DNA polymerases;Allaudeen;Antiviral Res.,1982
2. Selective inhibition of DNA replication in herpes simplex virus infected cells by 1-(2′-deoxy-2′-fluoro-β-d-arabinofuranosyl)-5-iodo-cytosine;Allaudeen;J. Biol. Chem.,1982
3. On the mechanism of selective inhibition of herpes-virus replication by (E)-5-(2-bromovinyl)-2′-deoxyuridine;Allaudeen,1981
4. Incorporation of E-5-(2-halovinyl)-2′-deoxyuridine into deoxyribonucleic acids of herpes simplex virus type 1-infected cells;Allaudeen;J. Biol. Chem.,1982
5. Antiviral activity of arabinosylthymine in herpesviral replication: mechanism of action in vivo and in vitro;Aswell;Antimicrob. Agents Chemother,1977
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1. Unanticipated Risk in Clinical Research ∗ ∗The editors have included Dr. Stephen Straus'original unedited contribution, penned for the book's 2002 edition and published with minor modification in the second edition in 2007, to honor his memory. This is a classic and compelling chapter with a story that remains relevant today. References to regulation and guidelines may not be current. The editors have added current references as of the time of publication to the end of the chapter.;Principles and Practice of Clinical Research;2018
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